scholarly journals Organocatalysis and Beyond: Activating Reactions with Two Catalytic Species

Catalysts ◽  
2019 ◽  
Vol 9 (11) ◽  
pp. 928 ◽  
Author(s):  
Arianna Sinibaldi ◽  
Valeria Nori ◽  
Andrea Baschieri ◽  
Francesco Fini ◽  
Antonio Arcadi ◽  
...  

Since the beginning of the millennium, organocatalysis has been gaining a predominant role in asymmetric synthesis and it is, nowadays, a foundation of catalysis. Synergistic catalysis, combining two or more different catalytic cycles acting in concert, exploits the vast knowledge acquired in organocatalysis and other fields to perform reactions that would be otherwise impossible. Merging organocatalysis with photo-, metallo- and organocatalysis itself, researchers have ingeniously devised a range of activations. This feature review, focusing on selected synergistic catalytic approaches, aims to provide a flavor of the creativity and innovation in the area, showing ground-breaking examples of organocatalysts, such as proline derivatives, hydrogen bond-mediated, Cinchona alkaloids or phosphoric acids catalysts, which work cooperatively with different catalytic partners.

Synthesis ◽  
2016 ◽  
Vol 49 (01) ◽  
pp. 167-174
Author(s):  
Ramon Rios ◽  
Kaiheng Zhang ◽  
Marta Meazza ◽  
Anabel Izaga ◽  
Clotilde Contamine ◽  
...  

Molecules ◽  
2020 ◽  
Vol 25 (2) ◽  
pp. 401 ◽  
Author(s):  
Franz Steppeler ◽  
Dominika Iwan ◽  
Elżbieta Wojaczyńska ◽  
Jacek Wojaczyński

For almost 20 years, thioureas have been experiencing a renaissance of interest with the emerged development of asymmetric organocatalysts. Due to their relatively high acidity and strong hydrogen bond donor capability, they differ significantly from ureas and offer, appropriately modified, great potential as organocatalysts, chelators, drug candidates, etc. The review focuses on the family of chiral thioureas, presenting an overview of the current state of knowledge on their synthesis and selected applications in stereoselective synthesis and drug development.


ChemInform ◽  
2012 ◽  
Vol 43 (17) ◽  
pp. no-no
Author(s):  
Michelangelo Gruttadauria ◽  
Francesco Giacalone ◽  
Renato Noto

2018 ◽  
Vol 14 ◽  
pp. 309-317 ◽  
Author(s):  
Lingjun Xu ◽  
Shuwen Han ◽  
Linjie Yan ◽  
Haifeng Wang ◽  
Haihui Peng ◽  
...  

A family of novel chloramphenicol base-amide organocatalysts possessing a NH functionality at C-1 position as monodentate hydrogen bond donor were developed and evaluated for enantioselective organocatalytic alcoholysis of meso-cyclic anhydrides. These structural diversified organocatalysts were found to induce high enantioselectivity in alcoholysis of anhydrides and was successfully applied to the asymmetric synthesis of (S)-GABOB.


2012 ◽  
Vol 124 (35) ◽  
pp. 8984-8988 ◽  
Author(s):  
Jorge Hernández-Toribio ◽  
Silvia Padilla ◽  
Javier Adrio ◽  
Juan C. Carretero

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